potassium chloride extended-release

Generic: potassium chloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-057
Product ID 82804-057_d0ce0bdf-5f24-4093-813f-881c61d7fcc7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209688
Listing Expiration 2026-12-31
Marketing Start 2023-04-10

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804057
Hyphenated Format 82804-057

Supplemental Identifiers

RxCUI
198116
UPC
0382804057306
UNII
660YQ98I10

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride extended-release (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA209688 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-90)
source: ndc

Packages (3)

82804-057-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-30) 82804-057-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-60) 82804-057-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-90)

Ingredients (1)

potassium chloride (1500 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d0ce0bdf-5f24-4093-813f-881c61d7fcc7", "openfda": {"upc": ["0382804057306"], "unii": ["660YQ98I10"], "rxcui": ["198116"], "spl_set_id": ["d0ce0bdf-5f24-4093-813f-881c61d7fcc7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-30)", "package_ndc": "82804-057-30", "marketing_start_date": "20240115"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-60)", "package_ndc": "82804-057-60", "marketing_start_date": "20240115"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-90)", "package_ndc": "82804-057-90", "marketing_start_date": "20240115"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "82804-057_d0ce0bdf-5f24-4093-813f-881c61d7fcc7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "82804-057", "generic_name": "Potassium Chloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA209688", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}